Canonical Allele Identifier: CA1732852164
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893264_107893265delinsAC , CM000669.2:g.107893264_107893265delinsAC GRCh38
NC_000007.13:g.107533709_107533710delinsAC , CM000669.1:g.107533709_107533710delinsAC GRCh37
NC_000007.12:g.107320945_107320946delinsAC NCBI36
NG_008045.1:g.7124_7125delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.104_105delinsAC MANE Select ENSP00000205402.3:p.Tyr35=
ENST00000639772.1:c.104_105delinsAC ENSP00000492159.1:p.Tyr35=
ENST00000205402.9:c.104_105delinsAC ENSP00000205402.3:p.Tyr35=
ENST00000415325.5:c.104_105delinsAC ENSP00000402593.1:p.Tyr35=
ENST00000417551.5:c.104_105delinsAC ENSP00000390667.1:p.Tyr35=
ENST00000437604.6:c.104_105delinsAC ENSP00000387542.2:p.Tyr35=
ENST00000440410.5:c.104_105delinsAC ENSP00000417016.1:p.Tyr35=
ENST00000450038.5:c.104_105delinsAC ENSP00000409590.1:p.Tyr35=
ENST00000451081.5:c.104_105delinsAC ENSP00000388077.1:p.Tyr35=
ENST00000453354.5:n.169_170delinsAC
ENST00000460577.5:n.138_139delinsAC
ENST00000485066.1:n.193_194delinsAC
ENST00000494441.1:n.249_250delinsAC
NM_000108.4:c.104_105delinsAC NP_000099.2:p.Tyr35=
NM_001289750.1:c.-45_-44delinsAC NP_001276679.1:n.-45_-44delinsAC
NM_001289751.1:c.104_105delinsAC NP_001276680.1:p.Tyr35=
NM_001289752.1:c.104_105delinsAC NP_001276681.1:p.Tyr35=
NM_000108.5:c.104_105delinsAC MANE Select NP_000099.2:p.Tyr35=